Butanal → Formate
Reaction equation
[CH:1]([O-:3])=[O:2].[CH:4](=[O:8])[CH2:5][CH2:6][CH3:7].[CH2:9]=[O:10]>>[CH2:4]([C:5]([CH2:1][OH:3])([CH2:9][OH:10])[CH2:6][CH3:7])[OH:8].[CH:1]([O-:3])=[O:2]Participants
5
Procedure
In the process of the invention, n-butyraldehyde is firstly reacted with formaldehyde in the presence of a base. This reaction can be carried out in one or more stages. In the single-stage variant, the starting materials are reacted directly to form trimethylolpropane and a formate salt. In a two-stage variant, n-butyraldehyde and formaldehyde are firstly reacted in the presence of catalytic amounts of base to form 2,2-dimethylolbutanal, purification or separation steps are carried out if desired and only then is the 2,2-dimethylolbutanal reacted with further formaldehyde in the presence of stoichiometric amounts of base to form trimethylolpropane and formate salt.
Workup
- customto form
- custom2,2-dimethylolbutanal, purification or separation steps
- customreacted with further formaldehyde in the presence of stoichiometric amounts of base
Sources & evidence
- ORD record
- ord-aa8dfbb3fb5d424bb2bb06948722cbea
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06448455B1
Reaction notes
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